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Activation Energy Calculator

Extract Ea from two experimental data points.

Activation energy from rate constants at two temperatures

The two-point Arrhenius form recovers Ea from how much the rate constant changes between two temperatures. No knowledge of A is needed.

k1 at T1k2 at T2Rate increaseActivation energy
0.05 at 320 K0.15 at 340 K3x49.7 kJ/mol
0.01 at 300 K0.02 at 310 K2x53.6 kJ/mol
0.001 at 298.15 K0.01 at 328.15 K10x62.4 kJ/mol
2 at 500 K8 at 550 K4x63.4 kJ/mol
1 x 10^-5 at 280 K1 x 10^-3 at 320 K100x85.8 kJ/mol

Most ordinary reactions fall between 40 and 100 kJ/mol. The second row is the classic case where a 10 degree rise doubles the rate, which corresponds to roughly 50 kJ/mol near room temperature.

The two-point form of the Arrhenius equation

Measuring a reaction's rate constant at two different temperatures lets you solve directly for activation energy, without ever needing to know the pre-exponential factor A.

A standard lab technique

This two-temperature method is exactly how activation energies are measured experimentally — run the same reaction at two temperatures, time it, and solve for Ea from the rate constants.

Frequently asked questions

My rate constant is 0.015 s⁻¹ at 300 K and 0.190 s⁻¹ at 350 K — what is the activation energy?

Ea = R × ln(k2/k1) / (1/T1 - 1/T2) = 8.314 × ln(0.190/0.015) / (1/300 - 1/350) = 8.314 × 2.54 / 4.76×10⁻⁴ ≈ 44,400 J/mol ≈ 44.4 kJ/mol.

How is this different from the Arrhenius equation calculator?

The Arrhenius calculator finds k from known Ea. This calculator works in reverse — given two rate constants at two temperatures, it extracts Ea without needing the pre-exponential factor A.

Why do I need two temperatures?

One rate constant at one temperature gives a single equation with two unknowns (Ea and A). Two temperatures provide two equations, eliminating A and isolating Ea. More data points improve precision.

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Last updated: September 7, 2026